Canonical Allele Identifier: CA2201615399

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362808C= , CM000678.2:g.1362808C=	GRCh38
NC_000016.9:g.1412809C= , CM000678.1:g.1412809C=	GRCh37
NC_000016.8:g.1352810C=	NCBI36
NG_016985.1:g.15910C=
NG_033129.1:g.56897G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.841-17C=
ENST00000529110.2:c.826-17C=	ENSP00000435349.2:n.826-17C=
ENST00000529957.6:n.800-17C=
ENST00000683366.1:c.*474-17C=	ENSP00000507283.1:n.*474-17C=
ENST00000683887.1:c.790-17C=	ENSP00000506886.1:n.790-17C=
ENST00000684100.1:n.736-17C=
ENST00000684126.1:n.876-17C=
ENST00000684688.1:n.1367-17C=
ENST00000204679.9:c.742-17C= MANE Select	ENSP00000204679.4:n.742-17C=
ENST00000204679.8:c.742-17C=	ENSP00000204679.4:n.742-17C=
ENST00000527076.1:n.1965-17C=
ENST00000527168.5:n.909-17C=
ENST00000529957.5:n.841-17C=
NM_032520.4:c.742-17C=	NP_115909.1:n.742-17C=
XM_017023782.1:c.790-17C=	XP_016879271.1:n.790-17C=
XM_017023783.1:c.382-17C=	XP_016879272.1:n.382-17C=
NM_032520.5:c.742-17C= MANE Select	NP_115909.1:n.742-17C=